BARBUTI Peter

Main Referenced Co-authors

KRÜGER, Rejko (5)

ANTONY, Paul (3)

HANSS, Zoé (3)

MASSART, François (3)

Caldwell, Maeve A. (2)

Main Referenced Keywords

alpha-synuclein (2); VPS35 (2); A30P (1); CRISPR-Cas9 (1); DYT6 dystonia (1);

Main Referenced Unit & Research Centers

Griffith Institute for Drug Discovery (1)

Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group) (1)

Luxembourg Centre for Systems Biomedicine (LCSB): Developmental and Cellular Biology (Schwamborn Group) (1)

Main Referenced Disciplines

Biochemistry, biophysics & molecular biology (5)

Genetics & genetic processes (2)

Publications (total 7)

Search in publications

The most downloaded

101 downloads

Krüger, R., Cheng, F., Walter, M., Riess, O., Wassouf, Z., Hentrich, T., Schulze-Hentrich, J., Barbuti, P., Grundmann-Hauser, K., Ott, T., & Casadei, N. (2020). Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia. Journal of Molecular Neuroscience. doi:10.1007/s12031-020-01490-2 https://hdl.handle.net/10993/43879

The most cited

137 citations (WOS)

McGough, I. J., Steinberg, F., Jia, D., Barbuti, P. A., McMillan, K. J., Heesom, K. J., Caldwell, M. A., Billadeau, D. D., Rosen, M. K., & Cullen, P. J. (2014). Retromer Binding to FAM21 and the WASH Complex Is Perturbed by the Parkinson Disease-Linked VPS35(D620N) Mutation. Current Biology. doi:10.1016/j.cub.2014.06.024 https://hdl.handle.net/10993/17269

Zanin, M., Santos, B. F. R., Antony, P., Berenguer-Escuder, C., Larsen, S. B., Hanss, Z., Barbuti, P., Baumuratov, A., Grossmann, D., Capelle, C. M., Weber, J., Balling, R., Ollert, M., Krüger, R., Diederich, N. J., & He, F. (10 November 2020). Mitochondria interaction networks show altered topological patterns in Parkinson's disease. NPJ Systems Biology and Applications, 6 (1), 38. doi:10.1038/s41540-020-00156-4

https://hdl.handle.net/10993/45728

Peer Reviewed verified by ORBi

Hanss, Z., Larsen, S., Antony, P., Mencke, P., Massart, F., Jarazo, J., Schwamborn, J. C., Barbuti, P., Mellick, G., & Krüger, R. (2020). Mitochondrial and Clearance Impairment in p.D620N VPS35 Patient-Derived Neurons. Movement Disorders. doi:10.1002/mds.28365

https://hdl.handle.net/10993/46008

Peer Reviewed verified by ORBi

Larsen, S., Hanss, Z., Cruciani, G., Massart, F., Barbuti, P., Mellick, G., & Krüger, R. (2020). Induced pluripotent stem cell line (LCSBi001-A) derived from a patient with Parkinson's disease carrying the p.D620N mutation in VPS35. Stem Cell Research. doi:10.1016/j.scr.2020.101776

https://hdl.handle.net/10993/43432

Peer Reviewed verified by ORBi

Krüger, R., Cheng, F., Walter, M., Riess, O., Wassouf, Z., Hentrich, T., Schulze-Hentrich, J., Barbuti, P., Grundmann-Hauser, K., Ott, T., & Casadei, N. (2020). Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia. Journal of Molecular Neuroscience. doi:10.1007/s12031-020-01490-2

https://hdl.handle.net/10993/43879

Peer Reviewed verified by ORBi

Barbuti, P., Antony, P., Rodrigues Santos, B., Massart, F., Cruciani, G., Dording, C., Arias, J., Schwamborn, J. C., & Krüger, R. (2020). Using High-Content Screening to Generate Single-Cell Gene-Corrected Patient-Derived iPS Clones Reveals Excess Alpha-Synuclein with Familial Parkinson's Disease Point Mutation A30P. Cells, 9 (9). doi:10.3390/cells9092065

https://hdl.handle.net/10993/44932

Peer Reviewed verified by ORBi

McGough, I. J., Steinberg, F., Jia, D., Barbuti, P. A., McMillan, K. J., Heesom, K. J., Caldwell, M. A., Billadeau, D. D., Rosen, M. K., & Cullen, P. J. (2014). Retromer Binding to FAM21 and the WASH Complex Is Perturbed by the Parkinson Disease-Linked VPS35(D620N) Mutation. Current Biology. doi:10.1016/j.cub.2014.06.024

https://hdl.handle.net/10993/17269

Peer Reviewed verified by ORBi

Crompton, L. A., Byrne, M. L., Taylor, H., Kerrigan, T. L., Bru-Mercier, G., Badger, J. L., Barbuti, P. A., Jo, J., Tyler, S. J., Allen, S. J., Kunath, T., Cho, K., & Caldwell, M. A. (2013). Stepwise, non-adherent differentiation of human pluripotent stem cells to generate basal forebrain cholinergic neurons via hedgehog signaling. Stem Cell Research, 11 (3), 1206-1221. doi:10.1016/j.scr.2013.08.002

https://hdl.handle.net/10993/17270

Peer Reviewed verified by ORBi